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Second Department of Internal Medicine Kobe University School of Medicine | 論文
- Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy
- Corneal Disorders in KKAy Mouse : A Type 2 Diabetes Model
- 先天性全身性脂肪萎縮症の2乳児例
- A surviving case of papillorenal syndrome with the phenotype of Potter sequence
- 各種栄養素の経静脈投与によるPancreatic Polypeptide分泌反応 (膵・消化管ホルモン)
- Epigallocatechin gallate inhibits sphere formation of neuroblastoma BE(2)-C cells
- Contemporary retrotransposition of a novel non-coding gene induces exon-skipping in dystrophin mRNA
- Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center
- Insertion of the IL1RAPL1 gene into the duplication junction of the dystrophin gene